Education
Ph.D. in Cellular and Molecular Biology, Dijon, France, 2007
Current position
Molecular Biologist in Centre GF Leclerc, Dijon, France
Publications (since 2013)
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Thibaudin, M., Chaix, M., Boidot, R., Végran, F., Derangère, V., Limagne, E., Berger, H., Ladoire, S., Apetoh, L. and Ghiringhelli, F. (2016). Human ectonucleotidase-expressing CD25 Th17 cells accumulate in breast cancer tumors and exert immunosuppressive functions. Oncoimmunology 5(1): e1055444.
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Bruchard, M., Boidot, R., Ghiringhelli, F. and Végran, F. (2015). Transcriptome analysis of TH2 CD4(+) T cells differentiated from wild-type and NLRP3KO mice. Genom Data 5: 314-315.
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Bruchard, M., Rebé, C., Derangère, V., Togbé, D., Ryffel, B., Boidot, R., Humblin, E., Hamman, A., Chalmin, F., Berger, H., Chevriaux, A., Limagne, E., Apetoh, L., Vegran, F. and Ghiringhelli, F. (2015). The receptor NLRP3 is a transcriptional regulator of TH2 differentiation. Nat Immunol 16(8): 859-870.
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Schmitt, E., Végran, F., Chevrier, S., Burillier, L., Cadouot, M., Lizard-Nacol, S., Coudert, B., Fumoleau, P., Arnould, L. and Boidot, R. (2015). Transcriptional expression of 8 genes predicts pathological response to first-line docetaxel + trastuzumab-based neoadjuvant chemotherapy. BMC Cancer 15: 169.
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Végran, F., Apetoh, L. and Ghiringhelli, F. (2015). Th9 cells: a novel CD4 T-cell subset in the immune war against cancer. Cancer Res 75(3): 475-479.
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Derangère, V., Chevriaux, A., Courtaut, F., Bruchard, M., Berger, H., Chalmin, F., Causse, S. Z., Limagne, E., Végran, F., Ladoire, S., Simon, B., Boireau, W., Hichami, A., Apetoh, L., Mignot, G., Ghiringhelli, F. and Rébé, C. (2014). Liver X receptor beta activation induces pyroptosis of human and murine colon cancer cells. Cell Death Differ 21(12): 1914-1924.
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Végran, F., Berger, H., Boidot, R., Mignot, G., Bruchard, M., Dosset, M., Chalmin, F., Rébé, C., Dérangère, V., Ryffel, B., Kato, M., Prevost-Blondel, A., Ghiringhelli, F. and Apetoh, L. (2014). The transcription factor IRF1 dictates the IL-21-dependent anticancer functions of TH9 cells. Nat Immunol 15(8): 758-766.
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Végran, F. and Boidot, R. (2013). Survivin-3B promotes chemoresistance and immune escape by inhibiting caspase-8 and -6 in cancer cells. Oncoimmunology 2(11): e26328.
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Boidot, R., Végran, F. and Lizard-Nacol, S. (2014). Transcriptional regulation of the survivin gene. Mol Biol Rep 41(1): 233-240.
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Rébé, C., Végran, F., Berger, H. and Ghiringhelli, F. (2013). STAT3 activation: A key factor in tumor immunoescape. JAKSTAT 2(1): e23010.
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Végran, F., Mary, R., Gibeaud, A., Mirjolet, C., Collin, B., Oudot, A., Charon-Barra, C., Arnould, L., Lizard-Nacol, S. and Boidot, R. (2013). Survivin-3B potentiates immune escape in cancer but also inhibits the toxicity of cancer chemotherapy. Cancer Res 73(17): 5391-5401.
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Végran, F., Berger, H., Ghiringhelli, F. and Apetoh, L. (2013). Socs3 induction by PPARgamma restrains cancer-promoting inflammation. Cell Cycle 12(14): 2157-2158.
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Bugaut, H., Bruchard, M., Berger, H., Derangère, V., Odoul, L., Euvrard, R., Ladoire, S., Chalmin, F., Végran, F., Rébé, C., Apetoh, L., Ghiringhelli, F. and Mignot, G. (2013). Bleomycin exerts ambivalent antitumor immune effect by triggering both immunogenic cell death and proliferation of regulatory T cells. PLoS One 8(6): e65181.
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Berger, H., Végran, F., Chikh, M., Gilardi, F., Ladoire, S., Bugaut, H., Mignot, G., Chalmin, F., Bruchard, M., Derangère, V., Chevriaux, A., Rébé, C., Ryffel, B., Pot, C., Hichami, A., Desvergne, B., Ghiringhelli, F. and Apetoh, L. (2013). SOCS3 transactivation by PPARgamma prevents IL-17-driven cancer growth. Cancer Res 73(12): 3578-3590.
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Végran, F., Rebucci, M., Chevrier, S., Cadouot, M., Boidot, R. and Lizard-Nacol, S. (2013). Only missense mutations affecting the DNA binding domain of p53 influence outcomes in patients with breast carcinoma. PLoS One 8(1): e55103.
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Bruchard, M., Mignot, G., Derangère, V., Chalmin, F., Chevriaux, A., Végran, F., Boireau, W., Simon, B., Ryffel, B., Connat, J. L., Kanellopoulos, J., Martin, F., Rébé, C., Apetoh, L. and Ghiringhelli, F. (2013). Chemotherapy-triggered cathepsin B release in myeloid-derived suppressor cells activates the Nlrp3 inflammasome and promotes tumor growth. Nat Med 19(1): 57-64.
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Hervieu, A., Rébé, C., Végran, F., Chalmin, F., Bruchard, M., Vabres, P., Apetoh, L., Ghiringhelli, F. and Mignot, G. (2013). Dacarbazine-mediated upregulation of NKG2D ligands on tumor cells activates NK and CD8 T cells and restrains melanoma growth. J Invest Dermatol 133(2): 499-508.